Home / Brands / MEDLINE INDUSTRIES, LP - Northfield
MEDLINE INDUSTRIES, LP - Northfield Recalls
822 recalls on record · December 29, 2021 to October 1, 2025 · Drugs, Medical Devices
Recalls by year
21
22
23
24
25
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
November 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls CENTURION MEDICAL PRODUCTS NICU PICC INSERTION BUNDLE W/O, REF CVI4470. Convenience kit used in medical procedures.
Hazard: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
November 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE CVC BARRIER KIT, REF DYNJ80485. Convenience kit used in medical procedures.
Hazard: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
November 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE RADIOLOGY PROCEDURE PACK, REF DYNJ67150A. Convenience kit used in medical procedures.
Hazard: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
November 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE DENTAL PACK, REF DYNJ66983. Convenience kit used in medical procedures.
Hazard: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
November 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE LINQ TRAY, REF DYNJ65880A. Convenience kit used in medical/surgical procedures.
Hazard: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
November 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE LITHOTOMY, REF DYNJ50099C. Convenience kit used in medical/surgical procedures.
Hazard: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
November 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls BAUSCH + LOMB CATARACT PACK, REF VAL001CPMEA. Convenience kit used in surgical procedures.
Hazard: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
November 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls BAUSCH + LOMB CATARACT TRAY, REF LYN023FACTB. Convenience kit used in surgical procedures.
Hazard: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
November 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls BAUSCH + LOMB EYE MUSCLE, REF VAL036EMESB. Convenience kit used in surgical procedures.
Hazard: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
November 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls BAUSCH + LOMB CATARACT PACK, REF VAL009CTSGA. Convenience kit used in surgical procedures.
Hazard: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
November 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls BAUSCH + LOMB BASIC OPHTHALMIC PACK, REF LYN023BSBLB. Convenience kit used in surgical procedures.
Hazard: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
November 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls BAUSCH + LOMB PHACO PACK, REF LYN011PHNHD. Convenience kit used in surgical procedures.
Hazard: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
November 9, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls BAUSCH + LOMB EYE PACK, REF LYN003EYSPA. Convenience kit used in surgical procedures.
Hazard: Medline received complaints on some of the breather pouches with in the sterile surgical kits show openings in the seal.
November 2, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE PRE-OP CHG BATHING KIT Reorder #: P164756
Hazard: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit.
November 2, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE 24 BLOOD CLUTURE KIT, Reorder #: DYNDH1632
Hazard: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit.
November 2, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE BLOOD CLUTURE KIT, Reorder #: DYNDH1592
Hazard: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit.
November 2, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE PHERIPHERAL BLOOD CULTURE DRAW, Reorder #: DYNDH1561
Hazard: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit.
November 2, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE ADLT BLOOD CLUTURE COLLECT KIT, Reorder #: DYNDH1245
Hazard: Adult Blood Culture Collect kit and Pre-Op Changing Bathing Kit contain an incorrect expiration date on a component with the kit. CHG Solution with the Pre-Op Changing Bathing Kit and Bactec bottle plastic both have an expiration date that does not match the date listed on the kit.
October 26, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls CENTURION SnagFree Chest Tube insertion Tray, Reorder CHT545
Hazard: One lot of chest tube insertion trays, containing a silk suture component that is restricted to 1 cycle of sterilization, was processed though 2 cycles.
October 19, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls VENCLOSE, VENCLOSE PROCEDURE PACK, 7VM, REF VC-PPH-67A. Cardiovascular procedure convenience kit.
Hazard: Impacted Venclose Procedure Packs contain a 12cm introducer/sheath component, either component #128626 - SET INTRO 7FX12CM FITS 0.018 or component #137339 - SET INTRO 6.5FX12CM FITS 0.018, instead of a 7cm introducer/sheath, component #137340 - SET INTRO 6.5FX7CM FITS 0.018
October 5, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE CLEARPRO TRACH T-PIECE CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner c
Hazard: Potential for the suction catheter to come apart from the green connector near the thumb valve. The connector is coming apart from the assembled device when pulling the catheter out of the artificial airway in the patient suctioning process.
October 5, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE CLEARPRO TRACH DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 I
Hazard: Potential for the suction catheter to come apart from the green connector near the thumb valve. The connector is coming apart from the assembled device when pulling the catheter out of the artificial airway in the patient suctioning process.
October 5, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE CLEARPRO DOUBLE SWIVEL CLOSED SUCTION CATHETER, flat peel pouch EA, 10 EA per Inner Carton (IC), 20 EA/2 Inner c
Hazard: Potential for the suction catheter to come apart from the green connector near the thumb valve. The connector is coming apart from the assembled device when pulling the catheter out of the artificial airway in the patient suctioning process.
August 10, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE MICRO-KILL GERMICIDAL BLEACH WIPES, Model numbers MSC351420AN, MSC351420ANH, MSC351420ANZ, MSC351430A, MSC351430
Hazard: stability failure
July 6, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls Medline Pill Splitters; 1 each/box; 144 boxes/carton
Hazard: Product lid (which houses a blade) is coming unhinged from the base, thus exposing the blade.
June 8, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE Polyurethane Foam Bedside Cleaning Kit, REF DYK100FS
Hazard: Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.
June 8, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE Polyurethane Foam Bedside Cleaning Kit, REF DYK215FS
Hazard: Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.
June 8, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE Polyurethane Bedside Cleaning Kit, REF DYK500FSAW
Hazard: Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.
June 8, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE Polyurethane Foam Bedside Cleaning Kit, REF DYK500FS
Hazard: Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.
June 8, 2022Medical DevicesFDA
MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE Polyurethane Foam Enzymatic Cleaning Sponge, REF DYK1000TSE
Hazard: Sporadic reports were received of discoloration on the foam sponge on certain lots of the product, which has been identified as microbial contamination.